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The architecture
Your central data is defined by the quality “manager” and accessible for all your users.
Your studies can be based on each product line, and consolidate several types of hazards simultaneously (physical, microbiological, allergen, organoleptic...)
Action plans for compliance retrofitting are common to all your studies, and monitored directly by each responsible.
Alarms on study review dates are centralised, and are displayed when opening the programme.
Unlike a « word processor or spreadsheet », its architecture allows genuine information sharing, and homogenization of studies between your different users.